Miller YE - Search Results

1

Regional assignment of the polymorphic probe D3S3 to 3p14 by molecular hybridization.

Gerber MJ, Miller YE, Drabkin HA, Scoggin CH. Gerber MJ, et al. Among authors: miller ye. Cytogenet Cell Genet. 1986;42(1-2):72-4. doi: 10.1159/000132254. Cytogenet Cell Genet. 1986. PMID: 3720360

2

Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.

Gerber MJ, Drabkin HA, Firnhaber C, Miller YE, Scoggin CH, Smith DI. Gerber MJ, et al. Among authors: miller ye. Am J Hum Genet. 1988 Oct;43(4):442-51. Am J Hum Genet. 1988. PMID: 2902784 Free PMC article.

3

Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene.

Fisher JH, Miller YE, Sparkes RS, Bateman JB, Kimmel KA, Carey TE, Rodell T, Shoemaker SA, Scoggin CH. Fisher JH, et al. Among authors: miller ye. Somat Cell Mol Genet. 1984 Sep;10(5):455-64. doi: 10.1007/BF01534850. Somat Cell Mol Genet. 1984. PMID: 6089356 Free article.

4

Chromosome 3q (22-ter) encodes the human transferrin receptor.

Miller YE, Jones C, Scoggin C, Morse H, Seligman P. Miller YE, et al. Am J Hum Genet. 1983 Jul;35(4):573-83. Am J Hum Genet. 1983. PMID: 6309000 Free PMC article.

5

Two-dimensional electrophoresis of peptides from human-CHO cell hybrids containing human chromosome 21.

Scoggin CH, Paul S, Miller YE, Patterson D. Scoggin CH, et al. Among authors: miller ye. Somatic Cell Genet. 1983 Nov;9(6):687-97. doi: 10.1007/BF01539474. Somatic Cell Genet. 1983. PMID: 6658644

6

Human aminoacylase-1: cloning, regional assignment to distal chromosome 3p21.1, and identification of a cross-hybridizing sequence on chromosome 18.

Miller YE, Drabkin H, Jones C, Fisher JH. Miller YE, et al. Genomics. 1990 Sep;8(1):149-54. doi: 10.1016/0888-7543(90)90237-o. Genomics. 1990. PMID: 1707030

7

Somatic cell genetic approaches to Down's syndrome.

Patterson D, Jones C, Scoggin C, Miller YE, Graw S. Patterson D, et al. Among authors: miller ye. Ann N Y Acad Sci. 1982;396:69-81. doi: 10.1111/j.1749-6632.1982.tb26844.x. Ann N Y Acad Sci. 1982. PMID: 6217778

8

A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.

Gemmill RM, Varella-Garcia M, Smith DI, Erickson P, Golembieski W, Miller Y, Coyle-Morris J, Tommerup N, Drabkin HA. Gemmill RM, et al. Genomics. 1991 Sep;11(1):93-102. doi: 10.1016/0888-7543(91)90105-n. Genomics. 1991. PMID: 1662666

9

Angiogenic squamous dysplasia in bronchi of individuals at high risk for lung cancer.

Keith RL, Miller YE, Gemmill RM, Drabkin HA, Dempsey EC, Kennedy TC, Prindiville S, Franklin WA. Keith RL, et al. Among authors: miller ye. Clin Cancer Res. 2000 May;6(5):1616-25. Clin Cancer Res. 2000. PMID: 10815878

10

Correlative assessment of morphologic, immunophenotypic, and genetic changes in bronchial epithelium of tobacco smokers.

Franklin WA, Todd S, Gemmill RM, Drabkin HA, Cook R, Sorenson J, Folkvord J, Haney J, Low R, Parks T, Proudfoot S, Kennedy T, Miller YE. Franklin WA, et al. Among authors: miller ye. Chest. 1996 Mar;109(3 Suppl):26S. doi: 10.1378/chest.109.3_supplement.26s. Chest. 1996. PMID: 8598139 No abstract available.

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